Novel regulation of MHC class II function in B cells

被引:152
作者
Matsuki, Yohei
Ohmura-Hoshino, Mari
Goto, Eiji
Aoki, Masami
Mito-Yoshida, Mari
Uematsu, Mika
Hasegawa, Takanori
Koseki, Haruhiko
Ohara, Osamu
Nakayama, Manabu
Toyooka, Kiminori
Matsuoka, Ken
Hotta, Hak
Yamamoto, Akitsugu
Ishido, Satoshi
机构
[1] RIKEN, Lab Infect Immun, Res Ctr Allergy & Immunol, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] RIKEN, Lab Dev Genet, Res Ctr Allergy & Immunol, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[3] RIKEN, Lab Immunogenom, Res Ctr Allergy & Immunol, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[4] Kazusa DNA Res Inst, Chiba, Japan
[5] RIKEN, Plant Sci Ctr, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[6] Kyushu Univ, Fac Agr, Lab Plant Nutr, Higashi Ku, Fukuoka 812, Japan
[7] Kobe Univ, Div Microbiol, Dept Genome Sci, Grad Sch Med,Chuo Ku, Kobe, Hyogo, Japan
[8] Nagahama Inst Biosci & Technol, Fac Biosci, Nagahama, Japan
关键词
antigen presentation; B cell; MHC class II; traffic; ubiquitination;
D O I
10.1038/sj.emboj.7601556
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The presence of post-translational regulation of MHC class II ( MHC II) under physiological conditions has been demonstrated recently in dendritic cells (DCs) that potently function as antigen-presenting cells (APCs). Here, we report that MARCH-I, an E3 ubiquitin ligase, plays a pivotal role in the post-translational regulation of MHC II in B cells. MARCH-I expression was particularly high in B cells, and the forced expression of MARCH-I induced the ubiquitination of MHC II. In B cells from MARCH-I- deficient mice (MARCH-I KO), the half-life of surface MHC II was prolonged and the ubiquitinated form of MHC II completely disappeared. In addition, MARCH-I-deficient B cells highly expressed exogenous antigen-loaded MHC II on their surface and showed high ability to present exogenous antigens. These results suggest that the function of MHC II in B cells is regulated through ubiquitination by MARCH-I.
引用
收藏
页码:846 / 854
页数:9
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